NDC 0378-0032 – Metoprolol Tartrate

Metoprolol Tartrate 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0378-0032

Product details

Brand name
Metoprolol Tartrate
Generic name
Metoprolol tartrate
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076704
Marketed since
December 23, 1993
Listing expires
December 31, 2026
Pharmacologic class
beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Metoprolol Tartrate →

Package NDC codes (2)

Package NDCDescriptionSince
0378-0032-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-01)Dec 23, 1993
0378-0032-101000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0032-10)Dec 23, 1993

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